411 English-speaking jobs in Walloon Brabant

As Product Manager EMEA, you will manage a portfolio of RFID solutions, including readers, scanners, and tags. You will define product requirements, collaborate with teams to ensure commercial success, and lead commercialization strategies.

Process Engineer to design, optimize, and improve sterile fill and finish processes in the biotech or pharmaceutical industries. Lead NPI and technical transfer for new customer projects. Develop and execute validation strategies and process risk assessments.

The LPO & GET Lead for Computer System Validation (CSV) & Data Integrity (DI) will own site-level CSV/DI processes, ensuring compliance with regulatory requirements. The role requires deep understanding of CSV/DI in a pharma manufacturing environment, including 21CFR Part 11, EU Annex 11, and GAMP guidelines.

The LPO & GET Lead for Computer System Validation (CSV) & Data Integrity (DI) will own site-level CSV/DI processes, ensuring compliance with regulatory requirements. The role requires deep understanding of CSV/DI in a pharma manufacturing environment, including 21CFR Part 11, EU Annex 11, and GAMP guidelines.

Process Engineer to design, optimize, and improve sterile fill and finish processes in the biotech or pharmaceutical industries. Lead NPI and technical transfer for new customer projects. Develop and execute validation strategies and process risk assessments.

Part-time Quality Assurance Consultant to support growing biotech operations. Responsibilities include data management, information consolidation, supplier coordination, and Quality Agreement preparation. Requires 2+ years of relevant experience, strong communication skills, and a good command of English.

Experienced MSAT Quality Lead to support technology transfers, process validation, and quality troubleshooting for pharmaceutical projects. Strong GMP knowledge and proven experience in technology transfer, investigations, and CAPA lifecycle required.

Software Architect for the Beam component within the Proton-Therapy Business Unit. Define and maintain a robust, scalable software architecture. Contribute to solution phases, analyze problems, and identify technical risks. Support and coach developers, validate design choices, and ensure architectural coherence.

Senior Business Analyst to join a squad focused on Building & Facility Services in a large-scale Agile environment. Responsibilities include business analysis, requirements gathering, testing, documentation, and change management. Must have 5+ years of experience as a Business Analyst, fluency in English, and strong Agile methodology experience.

Senior Solution Data Architect needed to define and implement data solutions, ensuring alignment with Target Enterprise Architecture. Requires 3+ years of experience as a Data Architect with strong Azure data stack expertise (Databricks, Synapse, ADF, CosmosDB, Azure SQL, Azure API Management, Azure App Services, Azure Analysis Services). Fluent English required.

Bioanalytical Scientific Manager will design and execute bioanalytical strategies for biologics, small molecule, and gene therapy programs. Collaborate with cross-functional teams to translate study goals into analytical strategies and oversee bioanalytical activities.

Home Delivery Driver needed to provide excellent customer service and deliver shopping safely. Must have a full driving license (held for at least 3 years with no more than 6 points) and a positive, friendly attitude.

Senior Power BI Consultant will configure, tune, and optimize Power BI Server. Responsibilities include providing Level 2/3 support, managing incident and change processes, and designing and delivering Power BI dashboards. Requires a Bachelor's degree and at least 5 years of experience as a consultant on large-scale business application implementations. Minimum 5 years of experience with MS SQL Server, minimum 3 years with Power BI Report Server and Power BI Service, and minimum 3 years of Power BI development experience are required.

Ensures robust quality oversight of GxP-relevant digital systems, focusing on compliant implementation and control of computerized systems and data processes. Collaborates with QA teams, Clinical Operations, and stakeholders to ensure systems are fit-for-purpose, validated, and operated in accordance with regulatory expectations.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization initiatives.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization initiatives.

This role involves organizing and coordinating regulatory activities, supporting and coaching RA & QA Officers, and ensuring regulatory compliance. The successful candidate will manage information flow, provide regulatory support to customers, and contribute to the development of regulatory strategies.

Technical Service & Marketing Manager will execute tests on personal care formulations, interpret data, and collaborate with global technical teams. The role also involves identifying market trends, developing marketing strategies, and supporting sales through technical expertise and communication.

Revamp and transform the GMP/GDP Management Review process, evolving it into a forward-looking, proactive governance mechanism. This role involves reviewing current practices, identifying improvement opportunities, and designing future-state frameworks and processes. Requires 7-10 years of experience in Pharmaceutical Quality, Quality Systems, or related roles, with a minimum of 5-8 years working with Pharmaceutical Quality Management Systems (QMS). Strong experience with GMP/GDP and Management Review processes, and the ability to bridge strategy and operations are essential. Fluent English is mandatory.

Experienced MSAT Quality Lead to support technology transfers, process validation, and quality oversight for pharmaceutical projects. Strong QA expertise, operational experience, and excellent communication skills required.